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5-Ethyl-2-phenyl-2H-pyrazol-3-ylamine is a chemical compound belonging to the pyrazoles class, characterized by its nitrogen-rich aromatic rings. It features a phenyl ring, two nitrogen atoms, an ethyl group, and an amine group, which contribute to its unique structure and potential bioactivity. 5-ETHYL-2-PHENYL-2H-PYRAZOL-3-YLAMINE is primarily utilized in the fields of organic synthesis and pharmaceuticals, where it may exhibit various beneficial properties. However, further research is required to fully understand its specific applications, toxicity, and environmental impact.

1017781-37-1

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1017781-37-1 Usage

Uses

Used in Organic Synthesis:
5-Ethyl-2-phenyl-2H-pyrazol-3-ylamine is used as a building block in organic synthesis for the creation of various complex organic molecules. Its unique structure allows for versatile chemical reactions, making it a valuable component in the synthesis of pharmaceuticals, agrochemicals, and other specialty chemicals.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 5-Ethyl-2-phenyl-2H-pyrazol-3-ylamine is used as a key intermediate in the development of new drugs. Its nitrogen-rich structure and bioactive properties make it a promising candidate for the synthesis of novel therapeutic agents with potential applications in treating various diseases and medical conditions.
Used in Research and Development:
5-Ethyl-2-phenyl-2H-pyrazol-3-ylamine is utilized in research and development for the exploration of its potential bioactivity and pharmacological properties. Scientists and researchers investigate its interactions with biological targets, such as enzymes, receptors, and other proteins, to understand its potential therapeutic effects and mechanisms of action.
Used in Drug Design and Optimization:
5-ETHYL-2-PHENYL-2H-PYRAZOL-3-YLAMINE is employed in drug design and optimization processes to improve the efficacy, selectivity, and safety of drug candidates. Its unique structural features can be modified and fine-tuned to enhance the desired pharmacological properties and minimize potential side effects.
Used in Environmental and Toxicological Studies:
5-Ethyl-2-phenyl-2H-pyrazol-3-ylamine is also used in environmental and toxicological studies to assess its potential impact on ecosystems and human health. Researchers evaluate its stability, biodegradability, and ecotoxicity to ensure that its use in various applications does not pose significant risks to the environment or public health.

Check Digit Verification of cas no

The CAS Registry Mumber 1017781-37-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,1,7,7,8 and 1 respectively; the second part has 2 digits, 3 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1017781-37:
(9*1)+(8*0)+(7*1)+(6*7)+(5*7)+(4*8)+(3*1)+(2*3)+(1*7)=141
141 % 10 = 1
So 1017781-37-1 is a valid CAS Registry Number.

1017781-37-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-Ethyl-1-phenyl-1H-pyrazol-5-amine

1.2 Other means of identification

Product number -
Other names 5-ethyl-2-phenylpyrazol-3-amine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1017781-37-1 SDS

1017781-37-1Downstream Products

1017781-37-1Relevant articles and documents

Chiral Phosphoric Acid-Catalyzed Enantioselective Synthesis of Pyrazole-Based Unnatural α-Amino Acid Derivatives

Woldegiorgis, Alemayehu Gashaw,Han, Zhao,Lin, Xufeng

supporting information, p. 274 - 280 (2021/11/01)

An enantioselective synthesis of unnatural pyrazole-based α-chiral amino acid derivatives from the asymmetric reaction of N-aryl-5-aminopyrazoles with β,γ-alkynyl-α-imino esters using a chiral spirocyclic phosphoric acid catalyst was developed. Using the established methodology, various pyrazole-based α-amino acid derivatives with tetrasubstituted carbon stereocenters were obtained in 67–98% yields and with 73–99% enantioselectivities. The NH2 functionality in the corresponding products enables further transformations to a chiral thiourea and a lactam. (Figure presented.).

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